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dbVar

Database of genomic structural variation

nsv4891580

Organism: Homo sapiens

Study:nstd200 (Abel et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:6,711

Publication(s):Abel et al. 2020

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 146 SVs from 28 studies. See in: genome view

Submitted genomic201,928,994-201,935,745

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4891580	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	201,929,013 (-19, +19)	201,935,723 (-22, +22)
nsv4891580	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	201,898,141 (-19, +19)	201,904,851 (-22, +22)

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16425103	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16425103	Submitted genomic		NC_000001.11:g.(20 1928994_201929032) _(201935701_201935 745)del	GRCh38 (hg38)		NC_000001.11	Chr1	201,929,013 (-19, +19)	201,935,723 (-22, +22)
nssv16425103	Remapped	Perfect	NC_000001.10:g.(20 1898122_201898160) _(201904829_201904 873)del	GRCh37.p13	First Pass	NC_000001.10	Chr1	201,898,141 (-19, +19)	201,904,851 (-22, +22)

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv16425103	<0.001	3	29246

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